EP2891745B1 - Coated cloth and method for producing same - Google Patents
Coated cloth and method for producing same Download PDFInfo
- Publication number
- EP2891745B1 EP2891745B1 EP13833877.7A EP13833877A EP2891745B1 EP 2891745 B1 EP2891745 B1 EP 2891745B1 EP 13833877 A EP13833877 A EP 13833877A EP 2891745 B1 EP2891745 B1 EP 2891745B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fabric
- coated
- woven fabric
- resin
- air
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000004744 fabric Substances 0.000 title claims description 159
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000002759 woven fabric Substances 0.000 claims description 113
- 229920005989 resin Polymers 0.000 claims description 81
- 239000011347 resin Substances 0.000 claims description 81
- 239000000835 fiber Substances 0.000 claims description 43
- 239000011800 void material Substances 0.000 claims description 38
- 229920002994 synthetic fiber Polymers 0.000 claims description 34
- 239000012209 synthetic fiber Substances 0.000 claims description 33
- 238000012360 testing method Methods 0.000 claims description 33
- 238000010276 construction Methods 0.000 claims description 30
- 239000011248 coating agent Substances 0.000 claims description 19
- 238000000576 coating method Methods 0.000 claims description 19
- 229920001971 elastomer Polymers 0.000 claims description 17
- 239000000806 elastomer Substances 0.000 claims description 17
- 238000009941 weaving Methods 0.000 description 23
- 238000009991 scouring Methods 0.000 description 20
- 229920002050 silicone resin Polymers 0.000 description 19
- 238000004073 vulcanization Methods 0.000 description 18
- 229920002302 Nylon 6,6 Polymers 0.000 description 17
- 238000000034 method Methods 0.000 description 17
- -1 polyethylene terephthalate Polymers 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 229920002292 Nylon 6 Polymers 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 239000005751 Copper oxide Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 229910000431 copper oxide Inorganic materials 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000003058 platinum compounds Chemical class 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical group FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 238000006124 Pilkington process Methods 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HIHIPCDUFKZOSL-UHFFFAOYSA-N ethenyl(methyl)silicon Chemical compound C[Si]C=C HIHIPCDUFKZOSL-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/23—Inflatable members
- B60R21/235—Inflatable members characterised by their material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D1/00—Woven fabrics designed to make specified articles
- D03D1/02—Inflatable articles
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D11/00—Double or multi-ply fabrics not otherwise provided for
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
- D06N3/0006—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using woven fabrics
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/128—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with silicon polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/23—Inflatable members
- B60R21/235—Inflatable members characterised by their material
- B60R2021/23504—Inflatable members characterised by their material characterised by material
- B60R2021/23509—Fabric
- B60R2021/23514—Fabric coated fabric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/23—Inflatable members
- B60R21/235—Inflatable members characterised by their material
- B60R2021/23533—Inflatable members characterised by their material characterised by the manufacturing process
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/30—Flame or heat resistance, fire retardancy properties
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2203/00—Macromolecular materials of the coating layers
- D06N2203/06—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06N2203/066—Silicon polymers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2205/00—Condition, form or state of the materials
- D06N2205/20—Cured materials, e.g. vulcanised, cross-linked
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2211/00—Specially adapted uses
- D06N2211/12—Decorative or sun protection articles
- D06N2211/26—Vehicles, transportation
- D06N2211/268—Airbags
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2213/00—Others characteristics
- D06N2213/02—All layers being of the same kind of material, e.g. all layers being of polyolefins, all layers being of polyesters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3065—Including strand which is of specific structural definition
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3179—Woven fabric is characterized by a particular or differential weave other than fabric in which the strand denier or warp/weft pick count is specified
- Y10T442/3195—Three-dimensional weave [e.g., x-y-z planes, multi-planar warps and/or wefts, etc.]
- Y10T442/3203—Multi-planar warp layers
Definitions
- the present invention relates to a coated fabric suitable for air-bags.
- the present invention relates to a fabric useful for protecting the periphery of an opening, which is for connection with an inflator, in an air-bag main body.
- An air-bag device is a device to protect automobile occupants in the case of a collision of the automobile by inflating the air-bag instantly.
- the air-bag device usually includes: an inflator serving as a gas generator; and an air-bag made of a synthetic fabric designed to inflate with an inflator gas.
- the gas ejected from the inflator is very hot. Therefore, the periphery of an inflator connection opening, with which the hot gas makes direct contact, is treated to increase its heat resistance.
- Patent Document 1 a base fabric for an air-bag in the form of a bag, whose inlet for an inflator gas has increased heat resistance because a part of the air-bag for connection with the inflator is partially coated with a thick resin.
- Patent Document 1 a base fabric for an air-bag in the form of a bag, whose inlet for an inflator gas has increased heat resistance because a part of the air-bag for connection with the inflator is partially coated with a thick resin.
- this technique is to apply a light coating of resin to the entire surface of the base fabric and thereafter apply the second coating to a necessary part, and thus has a problem in that the coating has to be performed a plurality of times and this leads to increased costs.
- Patent Document 3 a method by which a reinforcing fabric or the like is polymerized on the periphery of an opening for connection with an inflator and the fabric is sewed on the periphery. This technique is to stack two reinforcing fabrics on the base fabric for an air-bag main body.
- the structure of the reinforcing fabric itself is not disclosed, and it is unknown whether the reinforcing fabric itself can withstand the high temperatures of the inflator gas currently used.
- Patent Document 1 JP-A-No. 2007-261380 ; Patent Document 2: JP-A-No. 2004-114981 ; Patent Document 3: JP-A-No. H8-225048 .
- EP-A-1770 191 discloses a hollow weave fabric for an air bag.
- EP-A-0866164 concerns a coated woven fabric.
- An object of the present invention is to provide a highly heat-resistant fabric that can reduce damage to a base fabric for an air-bag main body from a hot gas generated from an inflator.
- the present inventors have made a consideration in order to attain the above object and, as a result, found that it is possible to attain the object with the use of a coated fabric comprising a three dimensional construction woven fabric as defined in the accompanying claim 1.
- the invention thus provides:
- the present invention provides a coated fabric that can withstand a hot gas and that is suitable for air-bags.
- a coated fabric of the present invention includes, as a basic structure, a three dimensional construction woven fabric woven from fibers.
- the coated fabric is structured as illustrated in, for example, Fig. 1.
- Fig. 1 is a cross-sectional view of one example of a coated fabric 1.
- a three dimensional construction woven fabric 2 illustrated in Fig. 1 is a three-layer woven fabric, and is constituted of a plurality of fibers 3.
- the three dimensional construction woven fabric 2 is coated with an elastomer resin constituting an elastomer resin layer 4. In a space between the fibers, or, in some cases, in a space enclosed by the fibers and resin, there is a void 5 having an appropriate volume.
- Examples of the material for the fibers constituting the three dimensional construction woven fabric include synthetic fibers such as polyamide fibers, polyester fibers, aramid fibers, rayon fibers, polysulfone fibers, and ultra-high-molecular-weight polyethylene fibers. Of these, polyamide fibers and polyester fibers are preferable because of their excellent mass-producibility and economic efficiency.
- polyamide fibers examples include fibers made from: nylon 6; nylon 66; nylon 12; nylon 46; copolyamides of nylon 6 and nylon 66; copolyamides obtained by copolymerizing nylon 6 with a polyalkylene glycol, a dicarboxylic acid, an amine, or the like; or the like.
- Nylon 6 fibers and nylon 66 fibers are preferable because of their particularly excellent shock resistance.
- polyester fibers include fibers made from polyethylene terephthalate, polybutylene terephthalate, or the like. Fibers made from copolyesters obtained by copolymerizing polyethylene terephthalate or polybutylene terephthalate with isophthalic acid, 5-sodium sulfoisophthalic acid, or an aliphatic dicarboxylic acid such as adipic acid, which serves as an acid component, may also be used.
- Synthetic fibers may also contain one or more additives such as a heat stabilizer, an antioxidant, a photostabilizer, a lubricating agent, an antistatic agent, a plasticizer, a thickener, a pigment, and/or a flame retardant, for higher productivity in a spinning and drawing step and a processing step or for better properties.
- additives such as a heat stabilizer, an antioxidant, a photostabilizer, a lubricating agent, an antistatic agent, a plasticizer, a thickener, a pigment, and/or a flame retardant
- Warp and weft yarns of the three dimensional construction woven fabric of the present invention are preferably synthetic fibers of the same chemical structure. It is also preferable that the warp and weft yarns have the same total fineness and that the warp and weft yarns have the same single fiber fineness .
- Polymers of the same kind mean polymers having a common main repeating unit, such as nylon 66 polymers and polyethylene terephthalate polymers.
- a combination of a homopolymer and a copolymer is also acceptable as polymers of the same kind in the present invention.
- the polymers equally have, or equally do not have, the same kind of copolymer component in the same amount, such polymers are preferable also in terms of production management because the warp and weft yarns do not have to be handled as different yarns.
- the warp and weft yarns have the same total fineness or the same single fiber fineness
- the difference between total finenesses or the difference between single fiber finenesses is within 5% of the smaller one of the finenesses of the warp and weft yarns.
- the synthetic fibers for use in the present invention preferably have a total fineness of 100 to 700 dtex.
- Synthetic fibers having a total fineness of 100 dtex or greater are capable of keeping the strength of a woven fabric.
- the synthetic fibers have a small total fineness, the synthetic fibers have a low rigidity and therefore are prone to bend when forming a three dimensional construction woven fabric.
- Such synthetic fibers cannot keep voids and tend not to increase the void content.
- Synthetic fibers having a total fineness of 700 dtex or smaller are capable of keeping more suitable flexibility during storage and keeping a desirable void content.
- the total fineness is more preferably 300 to 650 dtex, even more preferably 400 to 600 dtex.
- the synthetic fibers having a total fineness within this range make it possible to achieve balanced improvements in strength, flexibility and void content of a woven fabric.
- the synthetic fibers are preferably synthetic fiber filaments having a relatively small single fiber fineness of 1 to 7 dtex. This is because a single fiber fineness of 1 dtex or greater makes it possible to produce synthetic fiber filaments without special arrangements, and a single fiber fineness of 7 dtex or smaller improves the flexibility of synthetic fiber filaments.
- the single fiber fineness is more preferably 2 to 6.8 dtex, even more preferably 3 to 6.6 dtex. Setting the single fiber fineness within the above-described low range is preferable, because it is possible to bring about the effect of reducing the rigidity of synthetic fiber filaments and thus improve the flexibility of a base fabric.
- the tensile strength of each of the single fibers constituting a coated fabric for an air-bag of the present invention is, for the purpose of satisfying the mechanical properties required of a woven fabric for an air-bag and in view of spinning operation, preferably 8.0 to 9.0 cN/dtex, more preferably 8.3 to 8.7 cN/dtex for both the warp and weft yarns.
- the coated fabric of the present invention has a void in a woven fabric.
- the percentage of the void is preferably 15 to 60%.
- Void content % Apparent mass ⁇ Actual mass / Acutal mass ⁇ 100
- the thickness of an uncoated base fabric and the thickness of a coated base fabric are found.
- the difference between the thicknesses of the uncoated base fabric and the coated base fabric is used as the thickness of a resin.
- the volume of the uncoated base fabric and the volume of the resin layer are found from a test piece, and the apparent mass is found from the density of fibers constituting the base fabric and the density of the resin which coats the base fabric. The apparent mass is calculated from the following equation.
- the void content is calculated from the obtained apparent mass and actual mass.
- the thickness of the uncoated base fabric is found in the following manner: a photograph of a cross section of the coated base fabric is taken with a scanning electron microscope, and the thickness of a base fabric portion, which is a three dimensional construction woven fabric, and the thickness of a resin portion are found.
- the density of the original yarn is found by picking out a fiber with no resin attached.
- the density of the resin is found by dissolving the original yarn in a solvent that dissolves the original yarn but does not dissolve the resin and using the remaining resin.
- An example of a solvent that dissolves nylon 66 is formic acid, and an example of a solvent that dissolves polyethylene terephthalate is hexafluoroisopropanol.
- the density can be found by method A (water replacement method), method B (pycnometer method), method C (sink-float method), or method D (density gradient tube method) of JIS K7112 (1999).
- test pieces in the form of a square measuring 20 cm ⁇ 20 cm are taken out from five positions and measured, and the mean of the void contents calculated using the test pieces is used.
- the coated fabric having a void content within the above range brings about the heat insulation effect and thus improves heat resistance.
- the coated fabric having a low void content cannot bring about a sufficient heat insulation effect, and the coated fabric having a high void content cannot keep the thickness as a fabric and has a tendency to have a crushed woven fabric structure. Therefore, the void content is more preferably 20% or higher, whereas the upper limit of the void content is 60% or lower, preferably 40% or lower.
- At least one surface of a woven fabric needs to be coated with an elastomer resin layer. This makes it possible to protect the woven fabric from a hot gas generated from an inflator.
- the elastomer resin for coating the woven fabric is preferably a heat-resistant, cold-resistant, and flame-resistant resin.
- the elastomer resin include silicone resins, polyamide resins, polyurethane resins, and fluororesins. Of these, silicone resins are particularly preferable in view of heat resistance and low air permeability.
- the silicone resins include dimethyl silicone resins, methylvinyl silicone resins, methylphenyl silicone resins, and fluoro silicone resins.
- the resin for coating the woven fabric contain a flame-resistant compound.
- the flame-resistant compound include: halogenated compounds containing bromine, chlorine, or the like; platinum compounds; antimony oxide; copper oxide; titanium oxide; phosphorus compounds; thiourea compounds; carbon; cerium; and silicon oxide.
- halogenated compounds in particular halogenated cycloalkanes, platinum compounds, copper oxide, titanium oxide, and carbon are more preferable.
- the amount of the resin for coating the woven fabric, which is applied to one surface of the woven fabric is 50 to 500 g/m 2 .
- the upper limit is preferably 400 g/m 2 or less, more preferably 300 g/m 2 or less, even more preferably 250 g/m 2 or less.
- the lower limit is preferably 100 g/m 2 or more.
- An amount of the resin within this range makes it possible to achieve both the heat resistance and flexibility of the coated fabric for an air-bag.
- the amount of the resin attached to the surface is 50 g/m 2 or more, it is possible to cover the surface of the woven fabric in a uniform manner and to achieve heat resistance and good followability to a connection part.
- the other surface of the three dimensional construction woven fabric does not have to be coated. Note, however, that the other surface is also preferably coated for improved heat resistance.
- the thickness is 500 g/m 2 or less, more preferably 200 g/m 2 or less, even more preferably 100 g/m 2 or less.
- the lower limit is preferably 50 g/m 2 or more. In the case where the amount of the resin attached to the other surface is equal to or smaller than the above-described level, it is possible to improve heat resistance and flexibility.
- the resin covers the surface of the woven fabric in a uniform manner, and it is possible to improve heat resistance and achieve flexibility and possible to enhance the heat insulation effect brought about by the void formed inside the three dimensional construction woven fabric.
- the coated fabric of the present invention preferably has a thickness of 0.5 to 2.5 mm, more preferably 0.7 to 2.3 mm, even more preferably 0.9 to 2.0 mm.
- the coated fabric having a thickness within the above range makes it possible to achieve both the heat resistance and flexibility required of a coated fabric for an air-bag.
- a three dimensional construction woven fabric of the present invention means a woven fabric that has fibers on its front surface and, in addition, in the woven fabric and/or on the other surface of the woven fabric, fibers running along the same direction as those on the front surface.
- the woven fabric is woven after its structure is designed so that the woven fabric will be a multilayer woven fabric.
- a multilayer woven fabric is categorized into a three-layer woven fabric, a four-layer woven fabric, a five-layer woven fabric, a six-layer woven fabric, and the like.
- a two-layer woven fabric cannot easily provide a necessary void content, and a five-layer woven fabric and a six-layer woven fabric require a larger amount of original yarns and this leads to increased costs. Therefore, of the above-listed woven fabrics, a three-layer woven fabric and a four-layer woven fabric are selected in the present invention.
- a warp yarn made from any of the foregoing materials and having any of the foregoing total finenesses is warped and put on a loom.
- a weft yarn is prepared in the same manner.
- the loom used may be a jacquard loom or a dobby loom.
- the three dimensional construction woven fabric is preferably woven with a dobby loom.
- the loom may be, for example, a water-jet loom, an air-jet loom, or a rapier loom.
- the woven fabric is subjected to processes such as scouring and heat setting.
- a coated fabric of the present invention is obtained by applying a resin to at least one surface of the three dimensional construction woven fabric.
- the resin may be applied with the use of a roll comma coater, a floating knife coater, a roll-on-knife coater, a reverse roll coater, a gravure roll coater, or the like.
- a roll comma coater is preferable.
- a floating knife coater is preferably used.
- the coated fabric described here can be produced very easily, and therefore has a cost advantage. Furthermore, the coated fabric has excellent heat resistance while keeping good mechanical properties specific to a three dimensional structure. In view of this, the coated fabric is suitable for use in air-bags, and even more suitable for use in a part that is to be attached to the periphery of an opening, which is for connection with an inflator, in an air-bag.
- the present invention will be described more specifically with reference to examples. It should be noted that, in the present invention, the effects of the invention were evaluated by evaluating the heat resistance of coated fabrics with the use of an inflator. This test is referred to as an inflation test. The method for performing the inflation test will be described later. Furthermore, the obtained coated fabrics were measured and evaluated by the following methods.
- the thickness was measured in accordance with JIS L 1096:1999 8.5 in the following manner: a pressure of 23.5 kPa was applied to a sample and, after the sample was left for 10 seconds to settle the thickness, the thickness was measured at each of five different positions of the sample, and the mean was calculated.
- the basis weight was measured in accordance with JIS L 1096:1999 8.4.2 by taking three test pieces of 20 cm ⁇ 20 cm and measuring the mass (g) of each of the test pieces.
- the mean of the masses was represented as a mass per 1 m 2 (g/m 2 ).
- a comparative sample which was prepared in the same manner except that no resin was applied, was measured.
- the basis weight of the comparative sample was measured in accordance with the section (2), and the difference between the basis weight of the coated fabric and the basis weight of the comparative sample was found as the amount of an attached elastomer resin (unit: g/m 2 ).
- the density of an original yarn was measured in accordance with JIS Z 8807, and the density of a resin to be used was measured in accordance with JIS K 6249.
- the thickness of an uncoated base fabric and the thickness of a coated base fabric were found in accordance with the section (1).
- the difference between the thicknesses of the uncoated base fabric and the coated base fabric was used as the thickness of a resin.
- the volume of the uncoated base fabric and the volume of the resin layer were found from a test piece, and the apparent mass was found from the density of the original yarn and the density of the resin. It should be noted that the test piece used in this example was in the shape of a square measuring 20 cm ⁇ 20 cm.
- the actual mass of the coated base fabric was found in accordance with the section (2), and the value obtained from the following equation was used as a void content.
- Void content % Apparent mass ⁇ Actual mass / Actual mass ⁇ 100 It should be noted that the density of a nylon 66 fiber used in the present invention was 1.14 g/cm 3 , the density of a polyethylene terephthalate fiber used in the present invention was 1.38 g/cm 3 , and the density of a silicone resin used in the present invention was 1.07 g/cm 3 .
- Fig. 2 conceptually illustrates a method for an inflation test.
- Fig. 2 (a) is a front view conceptually illustrating the test method
- Fig. 2 (b) is a cross-sectional view taken along line X-X' .
- Two coated fabrics 13 of the present invention were stacked together on the periphery of an exit gas port 11 of an inflator 10 on the inside of a fabric 12 for an air-bag main body, the inflator was ignited, and the coated fabrics and the fabric for an air-bag main body were checked for damage.
- the fabric for an air-bag main body has the following configuration.
- Warp and weft yarns used were twistless synthetic fiber filaments which are constituted of 136 nylon 66 filaments having a circular cross section and having a single fiber fineness of 3.46 dtex and which have a total fineness of 470 dtex, a strength of 8.5 cN/dtex, and a degree of elongation of 23%. From these synthetic fiber filaments, a woven fabric was woven so that the density of each of the warp and weft yarns would be 50 yarns per 2.54 cm.
- a surface of the woven fabric was coated with a solventless silicone resin having a viscosity of 50 Pa ⁇ s (50, 000 cP) so that the amount of the attached resin would be 25 g/m 2 , and a base fabric for a main body having a basis weight of 230 g/m 2 and a thickness of 0.33 mm was obtained.
- Warp and weft yarns used were twistless synthetic fiber filaments which are constituted of 72 nylon 66 filaments having a circular cross section and having a single fiber fineness of 6.53 dtex and which have a total fineness of 470 dtex, a strength of 8.5 cN/dtex, and a degree of elongation of 23%.
- a four-layer woven fabric in which the density of the warp yarn was 145 yarns per 2.54 cm and the density of the weft yarn was 105 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- the woven fabric was scoured and dried by a usual method, and was subsequently heat-set at 160°C for 1 minute with the use of a pin tenter dryer under dimensional restraint at a widthwise shrinkage rate of 0% and an overfeed rate of 0%.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 50 Pa ⁇ s (50,000 cP) with a roll comma coater so that the amount of the attached resin would be 240 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 60 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was measured and found to be 23%.
- the results obtained by measuring the woven fabric thickness and basis weight are shown in Table 1.
- the result of an inflation test on the coated fabric is shown in Table 1. As shown in Table 1, the coated fabric was highly heat-resistant.
- Example 2 The same synthetic fiber filaments as in Example 1 were used as warp and weft yarns.
- a four-layer woven fabric in which the density of the warp yarn was 145 yarns per 2.54 cm and the density of the weft yarn was 200 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 20 Pa ⁇ s (20,000 cP) with a roll comma coater so that the amount attached to the woven fabric would be 200 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 50 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was measured and found to be 15%.
- the result of an inflation test on the coated fabric is shown in Table 1. As shown in Table 1, the coated fabric was highly heat-resistant.
- Warp and weft yarns used were twistless synthetic fiber filaments which are constituted of 72 nylon 66 filaments having a circular cross section and having a single fiber fineness of 4.86 dtex and which have a total fineness of 350 dtex, a strength of 8.5 cN/dtex, and a degree of elongation of 23.4%.
- a four-layer woven fabric in which the density of the warp yarn was 165 yarns per 2.54 cm and the density of the weft yarn was 120 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 20 Pa ⁇ s (20,000 cP) with a roll comma coater so that the amount of the attached resin would be 250 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 50 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was measured and found to be 36%.
- the result of an inflation test on the coated fabric is shown in Table 1. As shown in Table 1, the coated fabric was highly heat-resistant.
- Example 3 The same synthetic fiber filaments as in Example 3 were used as warp and weft yarns.
- a four-layer woven fabric in which the density of the warp yarn was 165 yarns per 2.54 cm and the density of the weft yarn was 120 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 50 Pa ⁇ s (50,000 cP) with a roll comma coater so that the amount of the attached resin would be 300 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric for an air-bag was calculated and found to be 34%.
- the result of an inflation test on the coated fabric for an air-bag is shown in Table 1. As shown in Table 1, the coated fabric was highly heat-resistant.
- Warp and weft yarns used were twistless synthetic fiber filaments which are constituted of 96 polyethylene terephthalate filaments having a circular cross section and having a single fiber fineness of 5.83 dtex and which have a total fineness of 560 dtex, a strength of 7.5 cN/dtex, and a degree of elongation of 20%.
- a four-layer woven fabric in which the density of the warp yarn was 140 yarns per 2.54 cm and the density of the weft yarn was 100 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 50 Pa ⁇ s (50,000 cP) with a roll comma coater so that the amount of the attached resin would be 200 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 100 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was calculated and found to be 25%.
- the result of an inflation test on the coated fabric for an air-bag is shown in Table 1. As shown in Table 1, the coated fabric was highly heat-resistant.
- Example 2 The same synthetic fiber filaments as in Example 1 were used as warp and weft yarns.
- a three-layer woven fabric in which the density of the warp yarn was 100 yarns per 2.54 cm and the density of the weft yarn was 92 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless silicone resin having a viscosity of 50 Pa ⁇ s (50, 000 cP) with a roll comma coater so that the amount of the attached resin would be 200 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 50 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was calculated and found to be 17%.
- the result of an inflation test on the coated fabric is shown in Table 2. As shown in Table 2, as for this coated fabric, although the flame penetrated the first coated fabric and the second coated fabric was also damaged, the fabric for an air-bag main body was not affected.
- Example 2 The same synthetic fiber filaments as in Example 1 were used as warp and weft yarns.
- a four-layer woven fabric in which the density of the warp yarn was 120 yarns per 2.54 cm and the density of the weft yarn was 90 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless addition-type silicone resin having a viscosity of 50 Pa ⁇ s (50,000 cP) with a roll comma coater so that the amount of the attached resin would be 500 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 100 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric for an air-bag was calculated and found to be 15%.
- the result of an inflation test on the coated fabric is shown in Table 2. As shown in Table 2, the coated fabric was highly heat-resistant.
- Example 2 The same synthetic fiber filaments as in Example 1 were used as warp and weft yarns.
- a three-layer woven fabric in which the density of the warp yarn was 92 yarns per 2.54 cm and the density of the weft yarn was 92 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless silicone resin having a viscosity of 50 Pa ⁇ s (50, 000 cP) with a roll comma coater so that the amount of the attached resin (surface coating amount) would be 240 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount would be 60 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was calculated and found to be 6%.
- the result of an inflation test on the coated fabric is shown in Table 2. As shown in Table 2, as for this coated fabric, the flame penetrated the stack of two coated fabrics and the fabric for an air-bag main body was also damaged.
- Example 3 The same synthetic fiber filaments as in Example 3 were used as warp and weft yarns.
- a four-layer woven fabric in which the density of the warp yarn was 165 yarns per 2.54 cm and the density of the weft yarn was 120 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless silicone resin having a viscosity of 20 Pa ⁇ s (20, 000 cP) with a roll comma coater so that the amount of the attached resin would be 40 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric was obtained.
- the void content of the obtained coated fabric was calculated and found to be 32%.
- the result of an inflation test on the coated fabric for an air-bag is shown in Table 2. As shown in Table 2, as for this coated fabric, the flame penetrated the stack of two coated fabrics and the fabric for an air-bag main body was also damaged.
- Example 5 The same synthetic fiber filaments as in Example 5 were used as warp and weft yarns.
- a three-layer woven fabric in which the density of the warp yarn was 100 yarns per 2.54 cm and the density of the weft yarn was 100 yarns per 2.54 cm was woven with the use of a dobby loom.
- the warp yarn tension was controlled to 35 cN per yarn and the loom speed was 450 rpm.
- Example 1 the woven fabric was subjected to the same scouring and setting as in Example 1.
- the front surface of the woven fabric was coated with a solventless silicone resin having a viscosity of 50 Pa ⁇ s (50, 000 cP) with a roll comma coater so that the amount of the resin attached to the surface would be 100 g/m 2 , and thereafter was subjected to vulcanization at 190°C for 1 minute.
- the back surface of the woven fabric was coated with the same resin so that the amount of the attached resin would be 100 g/m 2 , and thereafter subjected to vulcanization at 190°C for 1 minute. In this way, a coated fabric for an air-bag was obtained.
- the void content of the obtained coated fabric for an air-bag was calculated and found to be 12%.
- the result of an inflation test on the coated fabric for an air-bag, which serves as a heat-resistant fabric, is shown in Table 2. As shown in Table 2, as for this coated fabric for an air-bag, the flame penetrated the stack of two coated fabrics and the fabric for an air-bag main body was also damaged.
- Example 1 Example 2
- Example 3 Example 4
- Example 5 Synthetic fiber Nylon 66 Nylon 66 Nylon 66 Nylon 66 Polyethylene terephthalate Total fineness dtex 470 470 350 350 560 Single yarn fineness dtex 6.53 6.53 4.86 4.86 5.83
- a coated fabric of the present invention is suitable for use as a base fabric for an air-bag which can reduce damage to an air-bag main body fabric from a hot gas generated from an inflator.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Air Bags (AREA)
- Woven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012187387 | 2012-08-28 | ||
JP2013008221 | 2013-01-21 | ||
PCT/JP2013/072730 WO2014034604A1 (ja) | 2012-08-28 | 2013-08-26 | コート布およびその製造方法 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2891745A1 EP2891745A1 (en) | 2015-07-08 |
EP2891745A4 EP2891745A4 (en) | 2016-05-18 |
EP2891745B1 true EP2891745B1 (en) | 2017-11-29 |
Family
ID=50183416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP13833877.7A Active EP2891745B1 (en) | 2012-08-28 | 2013-08-26 | Coated cloth and method for producing same |
Country Status (8)
Country | Link |
---|---|
US (1) | US9878684B2 (zh) |
EP (1) | EP2891745B1 (zh) |
JP (1) | JP6372081B2 (zh) |
KR (1) | KR101851050B1 (zh) |
CN (1) | CN104583486B (zh) |
BR (1) | BR112015004004A2 (zh) |
MX (1) | MX2015002395A (zh) |
WO (1) | WO2014034604A1 (zh) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014035948A1 (en) * | 2012-08-27 | 2014-03-06 | Airbag Technologies Llc | Heat resistant coating for use in airbags and methods of their manufacture |
EP3127759B1 (en) * | 2014-03-31 | 2019-02-06 | Toyobo Co., Ltd. | Coated fabric for airbag |
JP6513937B2 (ja) * | 2014-11-20 | 2019-05-15 | 住商エアバッグ・システムズ株式会社 | エアバッグ |
US10281248B2 (en) * | 2015-11-11 | 2019-05-07 | Northrop Grumman Innovation Systems, Inc. | Gas generators, launch tube assemblies including gas generators, and related systems and methods |
CN108883598B (zh) * | 2016-03-31 | 2020-05-19 | 东丽株式会社 | 层合体 |
US11752968B2 (en) * | 2017-03-31 | 2023-09-12 | Seiren Co., Ltd. | Non-coated air bag fabric and air bag |
US11752969B2 (en) * | 2017-09-29 | 2023-09-12 | Seiren Co., Ltd. | Non-coated air bag base cloth and air bag |
WO2019065894A1 (ja) * | 2017-09-29 | 2019-04-04 | セーレン株式会社 | ノンコートエアバッグ用織物およびエアバッグ |
US10800373B2 (en) * | 2017-12-06 | 2020-10-13 | Felters Of South Carolina, Llc | Vehicle safety devices and heat shields for use around inflators of automotive airbag systems and related methods |
US11492733B2 (en) * | 2020-02-21 | 2022-11-08 | Raytheon Technologies Corporation | Weave control grid |
KR102584297B1 (ko) * | 2020-12-29 | 2023-10-05 | 코오롱인더스트리 주식회사 | 이중 직물 및 이를 포함하는 물품 |
MX2023007708A (es) * | 2020-12-29 | 2023-07-10 | Kolon Inc | Tela bicapa y articulos que la comprenden. |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5846604A (en) | 1988-03-14 | 1998-12-08 | Nextec Applications, Inc. | Controlling the porosity and permeation of a web |
JPH02216342A (ja) * | 1989-02-17 | 1990-08-29 | Asahi Chem Ind Co Ltd | 袋織のエアーバッグ |
JPH03294542A (ja) * | 1990-01-09 | 1991-12-25 | Toray Ind Inc | 樹脂加工織物、その製造方法、エアバッグおよび帆布 |
JPH04159159A (ja) * | 1990-10-24 | 1992-06-02 | Asahi Chem Ind Co Ltd | 基布排気式エアーバッグ |
JP2949842B2 (ja) | 1990-11-29 | 1999-09-20 | 東レ株式会社 | エアーバッグ用布帛 |
JP3147239B2 (ja) * | 1991-09-13 | 2001-03-19 | エアバックス インターナショナル リミティド | 袋織エアバッグ |
GB2301320B (en) * | 1994-01-28 | 1998-03-11 | Asahi Chemical Ind | Air bag |
JPH08225048A (ja) | 1995-02-20 | 1996-09-03 | Toyo Tire & Rubber Co Ltd | 車両用エアバッグ |
GB9705524D0 (en) | 1997-03-18 | 1997-05-07 | Dow Corning | Coated textile fabrics |
JP2000326811A (ja) | 1999-05-21 | 2000-11-28 | Toyo Tire & Rubber Co Ltd | コート布の製造方法 |
AU5617300A (en) * | 1999-06-17 | 2001-01-09 | Milliken & Company | Two-layer coating system for airbag fabrics |
US6748980B2 (en) * | 2000-12-11 | 2004-06-15 | Toyo Boseki Kabushiki Kaisha | Base fabric for hollow-woven air bag and air bag |
JP2002314288A (ja) * | 2001-04-19 | 2002-10-25 | Seiren Co Ltd | 難燃性の導電性織物 |
JP3855775B2 (ja) * | 2002-01-16 | 2006-12-13 | 東レ株式会社 | コ−トエアバッグ用基布 |
JP2004114981A (ja) | 2002-09-30 | 2004-04-15 | Nippon Plast Co Ltd | エアバッグ |
JP4419378B2 (ja) * | 2002-10-04 | 2010-02-24 | 東レ株式会社 | エアバッグ用基布およびその製造方法 |
JP2004268880A (ja) * | 2003-03-12 | 2004-09-30 | Toyoda Gosei Co Ltd | エアバッグ |
JP2005105437A (ja) * | 2003-09-29 | 2005-04-21 | Asahi Kasei Fibers Corp | エアバッグ用袋織基布 |
US20050244596A1 (en) | 2004-04-30 | 2005-11-03 | Highland Industries, Inc. | Coated airbag fabric |
JP2005324646A (ja) * | 2004-05-13 | 2005-11-24 | Toyobo Co Ltd | インフレーターガス導入分配ホース |
JP4603297B2 (ja) * | 2004-06-07 | 2010-12-22 | 旭化成せんい株式会社 | ポリヘキサメチレンアジパミド繊維 |
EP1770191B1 (en) | 2004-07-16 | 2013-11-27 | Asahi Kasei Chemicals Corporation | Base cloth for hollow-woven air bag and method for production thereof |
JP2007261380A (ja) | 2006-03-28 | 2007-10-11 | Sumisho Airbag Systems Co Ltd | エアバッグ用基布及びその製造方法 |
CA2655825C (en) * | 2006-06-23 | 2015-02-03 | Toray Industries, Inc. | Woven fabric for air bags, air bags and process for production of the woven fabric for air bags |
JP4884192B2 (ja) | 2006-12-11 | 2012-02-29 | 住商エアバッグ・システムズ株式会社 | カーテンバッグ用ガス分配部材 |
EP2799602A3 (en) | 2007-12-28 | 2015-02-11 | Kolon Industries Inc. | An inflatable fabrics and an air-bag |
JP4800361B2 (ja) | 2008-09-05 | 2011-10-26 | アキレス株式会社 | 水密・気密性3次元構造布の製造方法 |
JP5126792B2 (ja) * | 2008-10-24 | 2013-01-23 | 平岡織染株式会社 | 高透光性膜材料 |
EP2610377B9 (en) * | 2010-08-23 | 2017-08-02 | Asahi Kasei Kabushiki Kaisha | Base fabric for airbag |
-
2013
- 2013-08-26 EP EP13833877.7A patent/EP2891745B1/en active Active
- 2013-08-26 CN CN201380045199.3A patent/CN104583486B/zh active Active
- 2013-08-26 WO PCT/JP2013/072730 patent/WO2014034604A1/ja active Application Filing
- 2013-08-26 US US14/419,627 patent/US9878684B2/en active Active
- 2013-08-26 MX MX2015002395A patent/MX2015002395A/es unknown
- 2013-08-26 BR BR112015004004A patent/BR112015004004A2/pt not_active Application Discontinuation
- 2013-08-26 KR KR1020157006146A patent/KR101851050B1/ko active IP Right Grant
- 2013-08-26 JP JP2013548121A patent/JP6372081B2/ja not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
None * |
Also Published As
Publication number | Publication date |
---|---|
BR112015004004A2 (pt) | 2017-07-04 |
CN104583486A (zh) | 2015-04-29 |
CN104583486B (zh) | 2016-06-01 |
KR20150048768A (ko) | 2015-05-07 |
JP6372081B2 (ja) | 2018-08-15 |
MX2015002395A (es) | 2015-06-03 |
WO2014034604A1 (ja) | 2014-03-06 |
US20150210240A1 (en) | 2015-07-30 |
JPWO2014034604A1 (ja) | 2016-08-08 |
EP2891745A1 (en) | 2015-07-08 |
KR101851050B1 (ko) | 2018-04-20 |
EP2891745A4 (en) | 2016-05-18 |
US9878684B2 (en) | 2018-01-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2891745B1 (en) | Coated cloth and method for producing same | |
EP3323919B1 (en) | Airbag base fabric, airbag and method of manufacturing airbag base fabric | |
EP3619078B1 (en) | Low permeability and high strength woven fabric and methods of making the same | |
EP3279377B1 (en) | Coated base fabric for airbag, airbag, and method for producing coated base fabric for airbag | |
EP3279376B1 (en) | Polyester base fabric for airbag, polyester airbag, and method for manufacturing polyester base fabric for airbag | |
EP2949797B1 (en) | Airbag fabric and airbag | |
EP3371357B1 (en) | Low permeability and high strength fabric and methods of making the same | |
EP2789715B1 (en) | Polyamide fiber and airbag fabric | |
EP2344366B1 (en) | Woven airbag fabric | |
EP3854919B1 (en) | Non-coated base fabric for airbag, airbag, and manufacturing method of non-coated base fabric for airbag | |
EP3418129A1 (en) | Bag body | |
JP4306392B2 (ja) | ノンコートエアバッグ用基布およびその製法 | |
JP3859038B2 (ja) | エアバッグ用織物 | |
EP3936647B1 (en) | Base fabric for airbag, and manufacturing method of base fabric for airbag | |
JP3888495B2 (ja) | エアバッグ用織物 | |
JP7533215B2 (ja) | エアバッグ用基布、エアバッグ用基布の製造方法およびエアバッグ | |
JP4574890B2 (ja) | エアバック用高密度織物 | |
CN110914491A (zh) | 气囊用织物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20150130 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
DAX | Request for extension of the european patent (deleted) | ||
RA4 | Supplementary search report drawn up and despatched (corrected) |
Effective date: 20160415 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: D06M 101/32 20060101ALI20160411BHEP Ipc: B05D 7/00 20060101ALI20160411BHEP Ipc: B60R 21/23 20060101ALI20160411BHEP Ipc: D03D 1/02 20060101ALI20160411BHEP Ipc: D06M 15/643 20060101AFI20160411BHEP Ipc: D06N 3/12 20060101ALI20160411BHEP Ipc: D03D 11/00 20060101ALI20160411BHEP Ipc: B60R 21/235 20060101ALI20160411BHEP Ipc: D06N 3/00 20060101ALI20160411BHEP Ipc: D06M 101/34 20060101ALI20160411BHEP |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
INTG | Intention to grant announced |
Effective date: 20170516 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
GRAL | Information related to payment of fee for publishing/printing deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR3 |
|
GRAR | Information related to intention to grant a patent recorded |
Free format text: ORIGINAL CODE: EPIDOSNIGR71 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
INTC | Intention to grant announced (deleted) | ||
INTG | Intention to grant announced |
Effective date: 20171019 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 950508 Country of ref document: AT Kind code of ref document: T Effective date: 20171215 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602013030197 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: RO Ref legal event code: EPE |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20171129 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 950508 Country of ref document: AT Kind code of ref document: T Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180228 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180301 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180228 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 6 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602013030197 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20180830 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180826 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180831 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180831 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20180831 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180831 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180826 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20180826 Ref country code: MK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20171129 Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20130826 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20171129 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20180329 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230515 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: RO Payment date: 20230712 Year of fee payment: 11 Ref country code: GB Payment date: 20230706 Year of fee payment: 11 Ref country code: CZ Payment date: 20230817 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20230703 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240702 Year of fee payment: 12 |